KR102379907B1 - 광학 필름 및 화상 표시 장치 - Google Patents
광학 필름 및 화상 표시 장치 Download PDFInfo
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- KR102379907B1 KR102379907B1 KR1020197022668A KR20197022668A KR102379907B1 KR 102379907 B1 KR102379907 B1 KR 102379907B1 KR 1020197022668 A KR1020197022668 A KR 1020197022668A KR 20197022668 A KR20197022668 A KR 20197022668A KR 102379907 B1 KR102379907 B1 KR 102379907B1
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- optical film
- resin
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- layer
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- 239000012788 optical film Substances 0.000 title claims abstract description 297
- 239000011347 resin Substances 0.000 claims abstract description 241
- 229920005989 resin Polymers 0.000 claims abstract description 241
- 239000010408 film Substances 0.000 claims abstract description 127
- 239000000758 substrate Substances 0.000 claims abstract description 44
- 238000003860 storage Methods 0.000 claims abstract description 35
- 239000010410 layer Substances 0.000 claims description 298
- 239000000203 mixture Substances 0.000 claims description 80
- 238000012360 testing method Methods 0.000 claims description 67
- 229920001721 polyimide Polymers 0.000 claims description 57
- 239000012790 adhesive layer Substances 0.000 claims description 46
- 239000011247 coating layer Substances 0.000 claims description 44
- 239000000463 material Substances 0.000 claims description 42
- 239000009719 polyimide resin Substances 0.000 claims description 20
- 229920006122 polyamide resin Polymers 0.000 claims description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 90
- 235000019589 hardness Nutrition 0.000 description 69
- 239000011248 coating agent Substances 0.000 description 59
- 238000000576 coating method Methods 0.000 description 59
- 238000002834 transmittance Methods 0.000 description 56
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 49
- 239000004642 Polyimide Substances 0.000 description 37
- 239000002585 base Substances 0.000 description 36
- 239000002245 particle Substances 0.000 description 34
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 33
- 239000002519 antifouling agent Substances 0.000 description 30
- 238000000034 method Methods 0.000 description 30
- 239000007787 solid Substances 0.000 description 30
- 230000003595 spectral effect Effects 0.000 description 28
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 26
- 239000000523 sample Substances 0.000 description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 25
- 239000000178 monomer Substances 0.000 description 25
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 24
- -1 polyethylene terephthalate Polymers 0.000 description 23
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 22
- 241000428199 Mustelinae Species 0.000 description 22
- 238000005259 measurement Methods 0.000 description 21
- 239000002904 solvent Substances 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 19
- 125000003118 aryl group Chemical group 0.000 description 18
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 16
- 239000012964 benzotriazole Substances 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 16
- 239000002184 metal Substances 0.000 description 16
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 16
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- 239000000377 silicon dioxide Substances 0.000 description 14
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 13
- 239000011521 glass Substances 0.000 description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 13
- UIIMBOGNXHQVGW-UHFFFAOYSA-N sodium;hydron;carbonate Chemical compound [Na+].OC(O)=O UIIMBOGNXHQVGW-UHFFFAOYSA-N 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 230000005865 ionizing radiation Effects 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 11
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 11
- 125000000524 functional group Chemical group 0.000 description 11
- 238000010438 heat treatment Methods 0.000 description 11
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- 238000010586 diagram Methods 0.000 description 10
- 229910052731 fluorine Inorganic materials 0.000 description 10
- 125000001153 fluoro group Chemical group F* 0.000 description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 9
- 150000004985 diamines Chemical class 0.000 description 9
- 230000035699 permeability Effects 0.000 description 9
- 238000010008 shearing Methods 0.000 description 9
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 8
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 8
- 230000005540 biological transmission Effects 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 125000004427 diamine group Chemical group 0.000 description 8
- 230000002349 favourable effect Effects 0.000 description 8
- 229920001296 polysiloxane Polymers 0.000 description 8
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 7
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 7
- 239000000975 dye Substances 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 239000011737 fluorine Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 6
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 6
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 230000003373 anti-fouling effect Effects 0.000 description 6
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 6
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 6
- 230000004927 fusion Effects 0.000 description 6
- 239000011342 resin composition Substances 0.000 description 6
- 229940042596 viscoat Drugs 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 239000004760 aramid Substances 0.000 description 5
- 229920003235 aromatic polyamide Polymers 0.000 description 5
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 5
- 230000001588 bifunctional effect Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000005520 cutting process Methods 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
- 239000005020 polyethylene terephthalate Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 4
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 4
- PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 4
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 4
- NVKGJHAQGWCWDI-UHFFFAOYSA-N 4-[4-amino-2-(trifluoromethyl)phenyl]-3-(trifluoromethyl)aniline Chemical group FC(F)(F)C1=CC(N)=CC=C1C1=CC=C(N)C=C1C(F)(F)F NVKGJHAQGWCWDI-UHFFFAOYSA-N 0.000 description 4
- 238000004833 X-ray photoelectron spectroscopy Methods 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 239000012965 benzophenone Substances 0.000 description 4
- 239000001055 blue pigment Substances 0.000 description 4
- 230000021615 conjugation Effects 0.000 description 4
- 239000006059 cover glass Substances 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- RZIPTXDCNDIINL-UHFFFAOYSA-N cyclohexane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCCC1(C(O)=O)C(O)=O RZIPTXDCNDIINL-UHFFFAOYSA-N 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 230000001678 irradiating effect Effects 0.000 description 4
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000035939 shock Effects 0.000 description 4
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 4
- RPOHXHHHVSGUMN-UHFFFAOYSA-N 1-n,4-n-bis(4-aminophenyl)benzene-1,4-dicarboxamide Chemical compound C1=CC(N)=CC=C1NC(=O)C1=CC=C(C(=O)NC=2C=CC(N)=CC=2)C=C1 RPOHXHHHVSGUMN-UHFFFAOYSA-N 0.000 description 3
- ZMPZWXKBGSQATE-UHFFFAOYSA-N 3-(4-aminophenyl)sulfonylaniline Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=CC(N)=C1 ZMPZWXKBGSQATE-UHFFFAOYSA-N 0.000 description 3
- WCXGOVYROJJXHA-UHFFFAOYSA-N 3-[4-[4-(3-aminophenoxy)phenyl]sulfonylphenoxy]aniline Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)S(=O)(=O)C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)=C1 WCXGOVYROJJXHA-UHFFFAOYSA-N 0.000 description 3
- APXJLYIVOFARRM-UHFFFAOYSA-N 4-[2-(3,4-dicarboxyphenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]phthalic acid Chemical group C1=C(C(O)=O)C(C(=O)O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(C(O)=O)C(C(O)=O)=C1 APXJLYIVOFARRM-UHFFFAOYSA-N 0.000 description 3
- HHLMWQDRYZAENA-UHFFFAOYSA-N 4-[4-[2-[4-(4-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropan-2-yl]phenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=C(C(C=2C=CC(OC=3C=CC(N)=CC=3)=CC=2)(C(F)(F)F)C(F)(F)F)C=C1 HHLMWQDRYZAENA-UHFFFAOYSA-N 0.000 description 3
- UTDAGHZGKXPRQI-UHFFFAOYSA-N 4-[4-[4-(4-aminophenoxy)phenyl]sulfonylphenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=C(S(=O)(=O)C=2C=CC(OC=3C=CC(N)=CC=3)=CC=2)C=C1 UTDAGHZGKXPRQI-UHFFFAOYSA-N 0.000 description 3
- XPAQFJJCWGSXGJ-UHFFFAOYSA-N 4-amino-n-(4-aminophenyl)benzamide Chemical compound C1=CC(N)=CC=C1NC(=O)C1=CC=C(N)C=C1 XPAQFJJCWGSXGJ-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- STZIXLPVKZUAMV-UHFFFAOYSA-N cyclopentane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCC1(C(O)=O)C(O)=O STZIXLPVKZUAMV-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
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- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 125000005647 linker group Chemical group 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000012860 organic pigment Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
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- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 2
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 2
- IYAZLDLPUNDVAG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 IYAZLDLPUNDVAG-UHFFFAOYSA-N 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- NBAUUNCGSMAPFM-UHFFFAOYSA-N 3-(3,4-dicarboxyphenyl)phthalic acid Chemical group C1=C(C(O)=O)C(C(=O)O)=CC=C1C1=CC=CC(C(O)=O)=C1C(O)=O NBAUUNCGSMAPFM-UHFFFAOYSA-N 0.000 description 2
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 2
- UITKHKNFVCYWNG-UHFFFAOYSA-N 4-(3,4-dicarboxybenzoyl)phthalic acid Chemical group C1=C(C(O)=O)C(C(=O)O)=CC=C1C(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 UITKHKNFVCYWNG-UHFFFAOYSA-N 0.000 description 2
- AIVVXPSKEVWKMY-UHFFFAOYSA-N 4-(3,4-dicarboxyphenoxy)phthalic acid Chemical group C1=C(C(O)=O)C(C(=O)O)=CC=C1OC1=CC=C(C(O)=O)C(C(O)=O)=C1 AIVVXPSKEVWKMY-UHFFFAOYSA-N 0.000 description 2
- AVCOFPOLGHKJQB-UHFFFAOYSA-N 4-(3,4-dicarboxyphenyl)sulfonylphthalic acid Chemical group C1=C(C(O)=O)C(C(=O)O)=CC=C1S(=O)(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 AVCOFPOLGHKJQB-UHFFFAOYSA-N 0.000 description 2
- FQEHXKKHEIYTQS-UHFFFAOYSA-N 4-[4-[2-[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl]-1,1,1,3,3,3-hexafluoropropan-2-yl]phenoxy]-3-(trifluoromethyl)aniline Chemical group FC(F)(F)C1=CC(N)=CC=C1OC1=CC=C(C(C=2C=CC(OC=3C(=CC(N)=CC=3)C(F)(F)F)=CC=2)(C(F)(F)F)C(F)(F)F)C=C1 FQEHXKKHEIYTQS-UHFFFAOYSA-N 0.000 description 2
- LACZRKUWKHQVKS-UHFFFAOYSA-N 4-[4-[4-amino-2-(trifluoromethyl)phenoxy]phenoxy]-3-(trifluoromethyl)aniline Chemical group FC(F)(F)C1=CC(N)=CC=C1OC(C=C1)=CC=C1OC1=CC=C(N)C=C1C(F)(F)F LACZRKUWKHQVKS-UHFFFAOYSA-N 0.000 description 2
- KIFDSGGWDIVQGN-UHFFFAOYSA-N 4-[9-(4-aminophenyl)fluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 KIFDSGGWDIVQGN-UHFFFAOYSA-N 0.000 description 2
- QHHKLPCQTTWFSS-UHFFFAOYSA-N 5-[2-(1,3-dioxo-2-benzofuran-5-yl)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)(C(F)(F)F)C(F)(F)F)=C1 QHHKLPCQTTWFSS-UHFFFAOYSA-N 0.000 description 2
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| KR102436547B1 (ko) * | 2017-09-29 | 2022-08-29 | 삼성디스플레이 주식회사 | 전자 장치 |
| CN111278643A (zh) | 2017-10-27 | 2020-06-12 | 应用材料公司 | 柔性盖板透镜膜 |
| KR102840830B1 (ko) | 2018-02-28 | 2025-08-01 | 다이니폰 인사츠 가부시키가이샤 | 광학 필름 및 화상 표시 장치 |
| JP2019152686A (ja) * | 2018-02-28 | 2019-09-12 | 大日本印刷株式会社 | 機能性フィルム、偏光板、および画像表示装置 |
| KR102547124B1 (ko) | 2018-03-30 | 2023-06-26 | 삼성디스플레이 주식회사 | 표시장치 |
| KR102635865B1 (ko) * | 2018-04-27 | 2024-02-14 | 다이니폰 인사츠 가부시키가이샤 | 광학 필름, 편광판 및 화상 표시 장치 |
| JP7716853B2 (ja) | 2018-05-10 | 2025-08-01 | アプライド マテリアルズ インコーポレイテッド | フレキシブルディスプレイ用の交換可能なカバーレンズ |
| KR102680576B1 (ko) | 2018-08-14 | 2024-07-01 | 어플라이드 머티어리얼스, 인코포레이티드 | 가요성 커버 렌즈용 다층 습식-건식 하드코트들 |
| JP2020030395A (ja) * | 2018-08-20 | 2020-02-27 | 住友化学株式会社 | 複合前面板及びその製造方法 |
| WO2020110966A1 (ja) * | 2018-11-27 | 2020-06-04 | 富士フイルム株式会社 | ハードコートフィルム、ハードコートフィルムを備えた物品、及び画像表示装置 |
| JP7572143B2 (ja) * | 2019-03-29 | 2024-10-23 | 大日本印刷株式会社 | 光学フィルムおよび画像表示装置 |
| KR102773740B1 (ko) * | 2019-06-21 | 2025-02-27 | 엘지디스플레이 주식회사 | 디스플레이 장치 |
| KR102606648B1 (ko) | 2019-06-26 | 2023-11-24 | 어플라이드 머티어리얼스, 인코포레이티드 | 폴더블 디스플레이들을 위한 플렉서블 다층 커버 렌즈 스택들 |
| US20220320475A1 (en) * | 2019-08-19 | 2022-10-06 | Boe Technology Group Co., Ltd. | Flexible display apparatus and fabrication method thereof |
| WO2021060560A1 (ja) * | 2019-09-27 | 2021-04-01 | 大日本印刷株式会社 | 樹脂層、光学フィルムおよび画像表示装置 |
| JP6858912B2 (ja) * | 2019-10-09 | 2021-04-14 | 日東電工株式会社 | フレキシブル画像表示装置およびそれに用いる光学積層体 |
| JP7198946B2 (ja) * | 2019-12-05 | 2023-01-04 | 富士フイルム株式会社 | 光学積層体、偏光板、画像表示装置、抵抗膜式タッチパネル及び静電容量式タッチパネル |
| KR102401803B1 (ko) * | 2019-12-27 | 2022-05-26 | 닛토덴코 가부시키가이샤 | 플렉서블 화상 표시 장치 및 그에 이용하는 광학 적층체 |
| CN113707007A (zh) * | 2020-05-21 | 2021-11-26 | 华为技术有限公司 | 一种显示面板和显示装置 |
| CN111862808A (zh) * | 2020-06-28 | 2020-10-30 | 京东方科技集团股份有限公司 | 显示盖板及其制备方法和柔性显示装置 |
| JP2024517120A (ja) | 2021-04-27 | 2024-04-19 | ダウ シリコーンズ コーポレーション | ヒドロシリル化反応硬化シリコーン感圧接着剤、組成物、及びその調製方法、並びにフレキシブル表示装置における使用方法 |
| JP7343721B2 (ja) | 2021-04-27 | 2023-09-12 | ダウ シリコーンズ コーポレーション | ラジカル硬化シリコーン感圧接着剤及び組成物、並びにその調製方法及びフレキシブルディスプレイデバイスにおける使用方法 |
| KR20240102976A (ko) | 2021-11-01 | 2024-07-03 | 다우 실리콘즈 코포레이션 | 실리콘 고무에 접착된 실리콘 감압성 접착제를 포함하는 적층 물품의 제조 방법 |
| KR20230092395A (ko) * | 2021-12-17 | 2023-06-26 | 엘지디스플레이 주식회사 | 표시장치 |
| WO2025206337A1 (ja) * | 2024-03-29 | 2025-10-02 | 東洋紡株式会社 | 光学フィルムおよび画像表示装置 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004311664A (ja) | 2003-04-04 | 2004-11-04 | Nitto Denko Corp | プラズマディスプレイ用直貼りフィルタ |
| JP2005314563A (ja) | 2004-04-28 | 2005-11-10 | Jsr Corp | 帯電防止フィルム |
| WO2010067857A1 (ja) | 2008-12-12 | 2010-06-17 | リンテック株式会社 | 積層体、その製造方法、電子デバイス部材および電子デバイス |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6312906A (ja) * | 1986-07-03 | 1988-01-20 | Oki Electric Ind Co Ltd | 膜厚測定方法 |
| JP2005002269A (ja) * | 2003-06-13 | 2005-01-06 | Three M Innovative Properties Co | 粘着テープ |
| US20090176077A1 (en) * | 2006-03-31 | 2009-07-09 | Dai Nippon Printing Co., Ltd. | Optical layered body |
| KR101632456B1 (ko) * | 2008-11-27 | 2016-06-21 | 가부시기가이샤 닛뽕쇼꾸바이 | 광학 필름과 그 제조 방법 |
| EP2551110B1 (en) * | 2011-07-29 | 2014-04-23 | Creator Technology B.V. | Impact resistant device comprising an optical layer |
| US9127915B1 (en) * | 2011-11-08 | 2015-09-08 | Novana, Inc. | Self-healing composites |
| JP5051328B1 (ja) * | 2012-01-27 | 2012-10-17 | 大日本印刷株式会社 | 光学積層体、偏光板及び画像表示装置 |
| KR101415839B1 (ko) * | 2012-08-23 | 2014-07-09 | 주식회사 엘지화학 | 하드코팅 필름 |
| JP6075009B2 (ja) * | 2012-10-31 | 2017-02-08 | Dic株式会社 | 加飾ハードコートフィルム及び加飾ハードコート粘着フィルム。 |
| KR101640631B1 (ko) * | 2012-12-12 | 2016-07-18 | 제일모직주식회사 | 편광판용 접착 필름, 이를 위한 접착제 조성물, 이를 포함하는 편광판 및 이를 포함하는 광학 표시 장치 |
| JPWO2014091759A1 (ja) * | 2012-12-14 | 2017-01-05 | コニカミノルタ株式会社 | 光学フィルムとその製造方法、円偏光板および有機el表示装置 |
| US9224980B2 (en) * | 2013-03-28 | 2015-12-29 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting device |
| KR101579645B1 (ko) * | 2013-04-10 | 2015-12-22 | 코오롱인더스트리 주식회사 | 폴리이미드 커버기판 |
| KR102085961B1 (ko) * | 2013-12-24 | 2020-03-06 | 엘지디스플레이 주식회사 | 플렉서블 유기 발광 표시 장치 및 플렉서블 유기 발광 표시 장치 제조 방법 |
| KR102314335B1 (ko) * | 2014-01-31 | 2021-10-19 | 도레이 카부시키가이샤 | 적층 필름 |
| JP6520104B2 (ja) * | 2014-12-18 | 2019-05-29 | 大日本印刷株式会社 | シーラントフィルム |
| KR20160083738A (ko) | 2015-01-02 | 2016-07-12 | 삼성전자주식회사 | 표시 장치용 윈도우 및 이를 포함하는 표시 장치 |
| JP2016193520A (ja) * | 2015-03-31 | 2016-11-17 | コニカミノルタ株式会社 | 透明積層フィルムおよびその製造方法 |
| US9789906B1 (en) | 2016-03-23 | 2017-10-17 | Ford Global Technologies, Llc | Twenty-eight-cornered strengthening member for vehicles |
| KR102752071B1 (ko) * | 2016-11-10 | 2025-01-10 | 삼성디스플레이 주식회사 | 표시 장치용 커버 윈도우 및 이를 포함하는 표시 장치 |
| KR102653753B1 (ko) * | 2016-11-16 | 2024-04-02 | 삼성디스플레이 주식회사 | 플렉서블 표시 장치용 윈도우 및 이를 포함하는 플렉서블 표시 장치 |
| US10033015B1 (en) * | 2017-04-07 | 2018-07-24 | Motorola Mobility Llc | Flexible, optically clear, composite structures for foldable displays in mobile devices |
-
2017
- 2017-12-28 WO PCT/JP2017/047350 patent/WO2018128171A1/ja not_active Ceased
- 2017-12-28 JP JP2018560398A patent/JPWO2018128171A1/ja active Pending
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-
2023
- 2023-12-28 JP JP2023222372A patent/JP2024050562A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004311664A (ja) | 2003-04-04 | 2004-11-04 | Nitto Denko Corp | プラズマディスプレイ用直貼りフィルタ |
| JP2005314563A (ja) | 2004-04-28 | 2005-11-10 | Jsr Corp | 帯電防止フィルム |
| WO2010067857A1 (ja) | 2008-12-12 | 2010-06-17 | リンテック株式会社 | 積層体、その製造方法、電子デバイス部材および電子デバイス |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2023239177A1 (ko) * | 2022-06-10 | 2023-12-14 | 주식회사 엘지화학 | 광학 디바이스 |
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| JP2024050562A (ja) | 2024-04-10 |
| JPWO2018128171A1 (ja) | 2019-11-21 |
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| JP2022095687A (ja) | 2022-06-28 |
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| TWI757400B (zh) | 2022-03-11 |
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